Final answer:
The Food and Drug Administration Amendments Act (FDAAA) of 2007 was the act that required drug products to be proven effective as part of the amendments to the Food, Drug, and Cosmetic Act (FDCA). It was implemented to ensure the safety and efficacy of drugs and to protect consumers from potentially harmful products. However, the strict regulations can pose challenges for some patients and small pharmaceutical companies.
Step-by-step explanation:
The act that required drug products to be proven effective as part of the amendments to the Food, Drug, and Cosmetic Act (FDCA) is the Food and Drug Administration Amendments Act (FDAAA) of 2007.
The FDA regulates the medicines that pharmacies are allowed to sell in the United States to ensure both safety and efficacy. This sometimes means a company has to test a drug for several years before it can reach the market. This legislation aimed to protect consumers from unsafe drugs that could potentially harm them.
While this protects the general public, there can be drawbacks for some groups, such as patients in need of immediate treatments or small pharma companies that struggle with the cost and time of the strict approval process.
Learn more about FDA Amendments Act (FDAAA) of 2007